Ganoderic acid H
IUPAC name: (2R,6S)-6-[(3S,5R,10S,12S,13R,14R,17R)-12-acetyloxy-3-hydroxy-4,4,10,13,14-pentamethyl-7,11,15-trioxo-1,2,3,5,6,12,16,17-octahydrocyclopenta[a]phenanthren-17-yl]-2-methyl-4-oxoheptanoic acid
CAS Number: 98665-19-1
Class: Terpenoid
Mushrooms contain this compound
1 mushrooms
MushID |
Thai name |
Common name |
Scientific name |
Family |
1 |
เห็ดหลินจือ |
Lingzhi |
Ganoderma lucidum ( Curtis ) P. Karst. |
Ganodermataceae |
2D Structure
Compound Properties
SMILES
O=C(CC(C(=O)O)C)CC(C1CC(=O)C2(C1(C)C(OC(=O)C)C(=O)C1=C2C(=O)CC2C1(C)CCC(C2(C)C)O)C)C
Physicochemical Properties
Formula |
C32H44O9 |
Molecular wieght(g/mol) |
572.69 |
Num. of Heavy atoms |
41 |
Num. of Aromatic Heavy atoms |
0 |
Fraction Csp3 |
0.75 |
Num. of Rotatable bonds |
8 |
Num. of H-bond acceptors |
9 |
Num. of H-bonds donors |
2 |
Molar Refractivity |
150.99 |
TPSA (square Angstrom) |
152.11 |
Lipophilicity
iLOGP |
2.54 |
XLOGP3 |
2.60 |
WLOGP |
3.88 |
MLOGP |
1.72 |
Silicos-IT LOGP |
5.25 |
Consensus LOGP |
3.20 |
Water Solubility
ESOL |
|
LogS |
-4.50 |
Solubility(mg/ml) |
1.81E-02 |
Solubility(mol/l) |
3.16E-05 |
Class |
Moderately soluble |
Ali |
|
LogS |
-5.44 |
Solubility(mg/ml) |
2.06E-03 |
Solubility(mol/l) |
3.60E-06 |
Class |
Moderately soluble |
Silicos-IT |
|
LogS |
-5.44 |
Solubility(mg/ml) |
2.08E-03 |
Solubility(mol/l) |
3.64E-06 |
Class |
Moderately soluble |
Pharmacokinetics
GI absorbtion |
Low |
BBB permeant |
No |
Pgp substrate |
Yes |
CYP1A2 inhibitor |
No |
CYP2C19 inhibitor |
No |
CYP2C9 inhibitor |
No |
CYP2D6 inhibitor |
No |
CYP3A4 inhibitor |
No |
Log Kp (skin permeation) (cm/s) |
-7.95 |
Druglikeness
Lipinski Num. violations |
1 |
Ghose Num. violations |
3 |
Veber Num. violations |
1 |
Egan Num. violations |
1 |
Muegge Num. violations |
1 |
Bioavailability Score |
0.11 |
Medicinal Chemistry
PAINS Num. of alerts |
0 |
Brenk Num. of alerts |
0 |
Leadlikeness Num. of violations |
2 |
Synthetic Accessibility |
6.60 |
Biological Activity
Biological Activity |
JID |
Antitumour |
6 |
Anti-angiogenic |
6 |
Anti-HIV |
6 |
Antihistaminic |
6 |
Anti hepatotoxic |
6 |
Complement inhibition |
6 |
Hypocholesterolemic |
6 |
Antiplatelet aggregation |
6 |